On the public citation graph
An auxin maximum in the middle layer controls stamen development and pollen maturation in Arabidopsis
0 signed · 146 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.devcel.2005.05.014openalex-snapshot
Plant Development Is Regulated by a Family of Auxin Receptor F Box Proteins
inferredcites →https://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
inferredcites →https://doi.org/10.1038/nature06215openalex-snapshot
Auxin transport is sufficient to generate a maximum and gradient guiding root growth
inferredcites →https://doi.org/10.1038/nature07875openalex-snapshot
A regulated auxin minimum is required for seed dispersal in Arabidopsis
inferredcites →https://doi.org/10.1038/ncb1009-1166openalex-snapshot
Receptor-like kinases shape the plant
inferredcites →https://doi.org/10.1038/ncomms1941openalex-snapshot
ER-localized auxin transporter PIN8 regulates auxin homeostasis and male gametophyte development in Arabidopsis
inferredcites →https://doi.org/10.1038/ncomms4855openalex-snapshot
The tapetal AHL family protein TEK determines nexine formation in the pollen wall
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01125.xopenalex-snapshot
The Arabidopsis MALE STERILITY1 (MS1) gene is a transcriptional regulator of male gametogenesis, with homology to the PHD‐finger family of transcription factors
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01644.xopenalex-snapshot
The Arabidopsis ABORTED MICROSPORES ( AMS ) gene encodes a MYC class transcription factor
inferredcites →https://doi.org/10.1093/aob/mcu042openalex-snapshot
New views of tapetum ultrastructure and pollen exine development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/err014openalex-snapshot
The final split: the regulation of anther dehiscence
inferredcites →https://doi.org/10.1093/jxb/eru365openalex-snapshot
Plasmodesmata in integrated cell signalling: insights from development and environmental signals and stresses
inferredcites →https://doi.org/10.1101/gad.1415106openalex-snapshot
Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.997902openalex-snapshot
The EXCESS MICROSPOROCYTES1 gene encodes a putative leucine-rich repeat receptor protein kinase that controls somatic and reproductive cell fates in the Arabidopsis anther
inferredcites →https://doi.org/10.1101/pdb.prot4943openalex-snapshot
Nonradioactive In Situ Hybridization of RNA Probes to Sections of Plant Tissues
inferredcites →https://doi.org/10.1104/pp.109.147025openalex-snapshot
VirtualPlant: A Software Platform to Support Systems Biology Research
inferredcites →https://doi.org/10.1105/tpc.010350openalex-snapshot
Multidrug Resistance –like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
inferredcites →https://doi.org/10.1105/tpc.105.036004openalex-snapshot
The NAC Transcription Factors NST1 and NST2 ofArabidopsisRegulate Secondary Wall Thickenings and Are Required for Anther Dehiscence
inferredcites →https://doi.org/10.1105/tpc.106.046391openalex-snapshot
Arabidopsis MYB26/MALE STERILE35Regulates Secondary Thickening in the Endothecium and Is Essential for Anther Dehiscence
inferredcites →https://doi.org/10.1105/tpc.107.057570openalex-snapshot
Auxin Regulates Arabidopsis Anther Dehiscence, Pollen Maturation, and Filament Elongation
inferredcites →https://doi.org/10.1105/tpc.109.071803openalex-snapshot
The ABORTED MICROSPORES Regulatory Network Is Required for Postmeiotic Male Reproductive Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.114.127282openalex-snapshot
The Cysteine Protease CEP1, a Key Executor Involved in Tapetal Programmed Cell Death, Regulates Pollen Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.11.2441openalex-snapshot
Multidrug Resistance-like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
inferredcites →https://doi.org/10.1105/tpc.9.11.1963openalex-snapshot
Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements.
inferredcites →https://doi.org/10.1111/j.0960-7412.2004.02064.xopenalex-snapshot
Expression of rolB in tobacco flowers affects the coordinated processes of anther dehiscence and style elongation
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02934.xopenalex-snapshot
ROX1, a gene induced by rolB, is involved in procambial cell proliferation and xylem differentiation in tobacco stamen
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03083.xopenalex-snapshot
Receptor‐like protein kinase 2 (RPK 2) is a novel factor controlling anther development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03254.xopenalex-snapshot
Transcription factor AtMYB103 is required for anther development by regulating tapetum development, callose dissolution and exine formation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03500.xopenalex-snapshot
Defective in Tapetal Development and Function 1 is essential for anther development and tapetal function for microspore maturation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03668.xopenalex-snapshot
ABCB19/PGP19 stabilises PIN1 in membrane microdomains in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05024.xopenalex-snapshot
Arabidopsis SMALL AUXIN UP RNA63 promotes hypocotyl and stamen filament elongation
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01271.xopenalex-snapshot
Changes in growth kinetics of stamen filaments cause inefficient pollination in massugu2, an auxin insensitive, dominant mutant of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1744-7909.2011.01078.xopenalex-snapshot
A Genetic Pathway for Tapetum Development and Function in Arabidopsis
inferredcites →https://doi.org/10.1111/jipb.12332openalex-snapshot
ABCB1 and ABCB19 auxin transporters have synergistic effects on early and late Arabidopsis anther development
inferredcites →https://doi.org/10.1111/tpj.12130openalex-snapshot
Auxin controls A rabidopsis anther dehiscence by regulating endothecium lignification and jasmonic acid biosynthesis
inferredcites →https://doi.org/10.1111/tpj.12694openalex-snapshot
DYT 1 directly regulates the expression of TDF 1 for tapetum development and pollen wall formation in A rabidopsis
inferredcites →https://doi.org/10.1111/tpj.12942openalex-snapshot
The DYT 1‐interacting proteins b HLH 010, b HLH 089 and b HLH 091 are redundantly required for A rabidopsis anther development and transcriptome
inferredcites →https://doi.org/10.1186/s12870-014-0278-3openalex-snapshot
MYB80 homologues in Arabidopsis, cotton and Brassica: regulation and functional conservation in tapetal and pollen development
inferredcites →https://doi.org/10.1242/dev.02463openalex-snapshot
Regulation of Arabidopsis tapetum development and function by DYSFUNCTIONAL TAPETUM1 ( DYT1 ) encoding a putative bHLH transcription factor
inferredcites →https://doi.org/10.1242/dev.030353openalex-snapshot
Auxin transport routes in plant development
inferredcites →https://doi.org/10.2307/3870557openalex-snapshot
Aux/IAA Proteins Repress Expression of Reporter Genes Containing Natural and Highly Active Synthetic Auxin Response Elements
inferredcites →https://doi.org/10.2307/3871586openalex-snapshot
Multidrug Resistance-Like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
inferredcites →https://doi.org/10.3389/fpls.2014.00333openalex-snapshot
Auxin polar transport in stamen formation and development: how many actors?
inferredcites →https://doi.org/10.3390/biom2020288openalex-snapshot
Leucine-Rich Repeat (LRR) Domains Containing Intervening Motifs in Plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4801124openalex-extracted
New Evidence of the Timing of Arsenic Accumulation, Expression of Arsenic-Response Genes and Phytoextraction Efficiency in Field-Grown Pteris Vittata Plants
inferred← citeshttps://doi.org/10.1002/ajb2.1463openalex-snapshot
The role of auxin in developmentally regulated programmed cell death in lace plant
inferred← citeshttps://doi.org/10.1002/nzc2.70027openalex-snapshot
Orchids Versus Model Plants: A Comparison of Flowering Mechanisms
inferred← citeshttps://doi.org/10.1007/124_2020_50openalex-snapshot
Crosstalk Between the Sporophyte and the Gametophyte During Anther and Ovule Development in Angiosperms
inferred← citeshttps://doi.org/10.1007/978-1-0716-3299-4_5openalex-snapshot
Hormones and Flower Development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-025-04714-0openalex-snapshot
Effect of high temperature on pollen grains and yield in economically important crops: a review
inferred← citeshttps://doi.org/10.1007/s00425-025-04716-yopenalex-snapshot
Overall explanation of auxin mechanisms that control vascular differentiation in leaves and organ development in flowers
inferred← citeshttps://doi.org/10.1007/s00497-021-00416-1openalex-snapshot
Evolution and diversity of the angiosperm anther: trends in function and development
inferred← citeshttps://doi.org/10.1007/s00709-017-1185-xopenalex-snapshot
ABA and IAA control microsporogenesis in Petunia hybrida L.
inferred← citeshttps://doi.org/10.1007/s11103-019-00836-8openalex-snapshot
Downregulation of the auxin transporter gene SlPIN8 results in pollen abortion in tomato
inferred← citeshttps://doi.org/10.1007/s11103-019-00911-0openalex-snapshot
A GARP transcription factor anther dehiscence defected 1 (OsADD1) regulates rice anther dehiscence
inferred← citeshttps://doi.org/10.1007/s11540-025-09878-6openalex-snapshot
Evaluation of Diploid Wild Potatoes Pollen Traits under Heat Stress
inferred← citeshttps://doi.org/10.1007/s11738-019-2835-8openalex-snapshot
Pollen development and function under heat stress: from effects to responses
inferred← citeshttps://doi.org/10.1007/s11816-019-00559-8openalex-snapshot
High daytime temperature induces male sterility with developmental defects in male reproductive organs of Arabidopsis
inferred← citeshttps://doi.org/10.1007/s12298-023-01377-7openalex-snapshot
MIR159 regulates multiple aspects of stamen and carpel development and requires dissection and delimitation of differential downstream regulatory network for manipulating fertility traits
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00004-1openalex-snapshot
CLAVATA signaling pathway receptors modulate developmental traits and stress responses in crops
inferred← citeshttps://doi.org/10.1016/j.cj.2024.04.010openalex-snapshot
A rice exocyst subunit gene SEC3A is required for anther dehiscence
inferred← citeshttps://doi.org/10.1016/j.cub.2022.02.073openalex-snapshot
Auxin boosts energy generation pathways to fuel pollen maturation in barley
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.119773openalex-snapshot
Arsenic accumulation in Pteris vittata: Time course, distribution, and arsenic-related gene expression in fronds and whole plantlets
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.124873openalex-snapshot
New evidence of the timing of arsenic accumulation and expression of arsenic-response genes in field-grown Pteris vittata plants under different arsenic concentrations
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144751openalex-snapshot
Auxin Response Factor 17 regulates Glycosylphosphatidylinositol-anchored Lipid Transfer Protein 4 for pollen tube elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119480openalex-snapshot
Multi-Omics analysis reveals the important role of indole-3-acetic acid homeostasis in male fertility of cotton
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.02.008openalex-snapshot
The Monochoria genome provides insights into the molecular mechanisms underlying floral heteranthery
inferred← citeshttps://doi.org/10.1016/j.molp.2026.03.016openalex-snapshot
Single-cell and haplotype-resolved transcriptomics reveal molecular signatures of orchid floral structures
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110645openalex-snapshot
Knockdown of the DUF647 family member RUS4 impairs stamen development and pollen maturation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109372openalex-snapshot
The DC1 domain protein Vacuoleless Gametophytes regulates stamen development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109393openalex-snapshot
Transcriptome and phytohormone profiling of stamen and pistil in Brassica napus under boron deficiency
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110393openalex-snapshot
Filament elongation and pollen development regulated by auxin is crucial for male fertility in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.sajb.2022.07.017openalex-snapshot
Comparative metabolomic analysis of unreleased and released pollen from Putranjiva roxburghii Wall.
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100914openalex-snapshot
Pollen development under control and high-temperature stress: the role of plant hormones
inferred← citeshttps://doi.org/10.1016/j.ygeno.2020.12.032openalex-snapshot
Comparative transcriptome analysis provides insight into the molecular mechanisms of anther dehiscence in eggplant (Solanum melongena L.)
inferred← citeshttps://doi.org/10.1038/s41477-018-0175-0openalex-snapshot
OsFTIP7 determines auxin-mediated anther dehiscence in rice
inferred← citeshttps://doi.org/10.1071/fp19215openalex-snapshot
Improved reproductive growth of euhalophyte Suaeda salsa under salinity is correlated with altered phytohormone biosynthesis and signal transduction
inferred← citeshttps://doi.org/10.1093/jxb/erac185openalex-snapshot
Arabidopsis TWISTED DWARF1 regulates stamen elongation by differential activation of ABCB1,19-mediated auxin transport
inferred← citeshttps://doi.org/10.1093/jxb/erad480openalex-snapshot
Environmental regulation of male fertility is mediated through Arabidopsis transcription factors bHLH89, 91, and 10
inferred← citeshttps://doi.org/10.1093/jxb/erae384openalex-snapshot
Imaging the spatial distribution of structurally diverse plant hormones
inferred← citeshttps://doi.org/10.1093/pcp/pcaa089openalex-snapshot
Letter to the Editor: The Role of Auxin in Late Stamen Development
inferred← citeshttps://doi.org/10.1093/pcp/pcx102openalex-snapshot
Auxin Response Dynamics During Wild-Type and entire Flower Development in Tomato
inferred← citeshttps://doi.org/10.1093/pcp/pcz127openalex-snapshot
Knockdown of Arabidopsis ROOT UVB SENSITIVE4 Disrupts Anther Dehiscence by Suppressing Secondary Thickening in the Endothecium
inferred← citeshttps://doi.org/10.1093/plcell/koac287openalex-snapshot
Anther development—The long road to making pollen
inferred← citeshttps://doi.org/10.1093/plcell/koag262openalex-snapshot
Cryptic fate priming and lineage stabilization during Arabidopsis anther development
inferred← citeshttps://doi.org/10.1093/plphys/kiae123openalex-snapshot
Tetrad stage transient cold stress skews auxin-mediated energy metabolism balance in Chinese cabbage pollen
inferred← citeshttps://doi.org/10.1093/plphys/kiag511openalex-snapshot
Anther middle layer fatty acid synthesis is essential for pollen development and fertility restoration at low temperature in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2021.11.30.470611openalex-snapshot
TWISTED DWARF1 regulates Arabidopsis stamen development by differential activation of ABCB-mediated auxin transport
inferred← citeshttps://doi.org/10.1101/cshperspect.a039974openalex-snapshot
Auxin and Flower Development: A Blossoming Field
inferred← citeshttps://doi.org/10.1104/pp.17.00719openalex-snapshot
Transcription Factor MYB26 Is Key to Spatial Specificity in Anther Secondary Thickening Formation
inferred← citeshttps://doi.org/10.1104/pp.19.00576openalex-snapshot
AUXIN RESPONSE FACTOR17 Directly Regulates MYB108 for Anther Dehiscence
inferred← citeshttps://doi.org/10.1104/pp.19.01501openalex-snapshot
Class-I TCP Transcription Factors Activate the SAUR63 Gene Subfamily in Gibberellin-Dependent Stamen Filament Elongation
inferred← citeshttps://doi.org/10.1105/tpc.16.00484openalex-snapshot
Carbonic Anhydrases Function in Anther Cell Differentiation Downstream of the Receptor-Like Kinase EMS1
inferred← citeshttps://doi.org/10.1105/tpc.17.00840openalex-snapshot
A Newly Identified Flower-Specific Splice Variant of AUXIN RESPONSE FACTOR8 Regulates Stamen Elongation and Endothecium Lignification in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.18.00074openalex-snapshot
Disrupted Genome Methylation in Response to High Temperature Has Distinct Affects on Microspore Abortion and Anther Indehiscence
inferred← citeshttps://doi.org/10.1111/jipb.12924openalex-snapshot
A novel CCCH‐type zinc finger protein SAW1 activates OsGA20ox3 to regulate gibberellin homeostasis and anther development in rice
inferred← citeshttps://doi.org/10.1111/nph.14790openalex-snapshot
Positive regulation of AMS by TDF1 and the formation of a TDF1–AMS complex are required for anther development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.15970openalex-snapshot
The long and short of the S ‐locus in Turnera (Passifloraceae)
inferred← citeshttps://doi.org/10.1111/nph.17878openalex-snapshot
Phytochrome interacting factor 3 regulates pollen mitotic division through auxin signalling and sugar metabolism pathways in tomato
inferred← citeshttps://doi.org/10.1111/nph.17939openalex-snapshot
The GA–DELLA–OsMS188 module controls male reproductive development in rice
inferred← citeshttps://doi.org/10.1111/nph.71462openalex-snapshot
Mitochondrial gene orf224 triggers retrograde signaling and reprogramming of anther cell fate in Brassica napus Polima CMS
inferred← citeshttps://doi.org/10.1111/pce.70842openalex-snapshot
OsNCED5 Controls Abscisic Acid‐Mediated Anther Dehiscence and Male Fertility in Rice
inferred← citeshttps://doi.org/10.1111/ppl.70340openalex-snapshot
Primary Auxin Response Genes GH3s and DAO1 Modulate Stamen Elongation in Arabidopsis thaliana and Solanum lycopersicum
inferred← citeshttps://doi.org/10.1111/tpj.14605openalex-snapshot
Mediator subunit OsMED14_1 plays an important role in rice development
inferred← citeshttps://doi.org/10.1111/tpj.14736openalex-snapshot
Light controls stamen elongation via cryptochromes, phytochromes and COP1 through HY5 and HYH
inferred← citeshttps://doi.org/10.1111/tpj.16089openalex-snapshot
The full‐length Auxin Response Factor 8 isoform ARF8 .1 controls pollen cell wall formation and directly regulates TDF1 , AMS and MS188 expression
inferred← citeshttps://doi.org/10.1111/tpj.70328openalex-snapshot
ARF10 , ARF16 , and ARF17 are involved in cytokinesis during pollen development in Arabidopsis
inferred← citeshttps://doi.org/10.1146/annurev-arplant-042817-040226openalex-snapshot
Essential Roles of Local Auxin Biosynthesis in Plant Development and in Adaptation to Environmental Changes
inferred← citeshttps://doi.org/10.1186/s12284-018-0219-0openalex-snapshot
Genome-wide analyses of late pollen-preferred genes conserved in various rice cultivars and functional identification of a gene involved in the key processes of late pollen development
inferred← citeshttps://doi.org/10.1186/s12864-020-07345-9openalex-snapshot
Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.1186/s12864-025-12297-zopenalex-snapshot
Comparative transcriptomic analysis of petaloid stamen formation in Lagerstroemia speciosa ‘Zijuan’
inferred← citeshttps://doi.org/10.1186/s12870-018-1571-3openalex-snapshot
Proline synthesis in developing microspores is required for pollen development and fertility
inferred← citeshttps://doi.org/10.1242/dev.174375openalex-snapshot
miR167 limits anther growth to potentiate anther dehiscence
inferred← citeshttps://doi.org/10.1360/ssv-2024-0051openalex-snapshot
Advance in the anther tapetum development and their regulatory mechanisms
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007397openalex-snapshot
Auxin production in diploid microsporocytes is necessary and sufficient for early stages of pollen development
inferred← citeshttps://doi.org/10.1371/journal.pone.0239230openalex-snapshot
Transcriptome sequencing and screening of genes related to sex determination of Trichosanthes kirilowii Maxim
inferred← citeshttps://doi.org/10.3389/fpls.2017.01735openalex-snapshot
Auxin Homeostasis in Arabidopsis Ovules Is Anther-Dependent at Maturation and Changes Dynamically upon Fertilization
inferred← citeshttps://doi.org/10.3389/fpls.2018.00150openalex-snapshot
SHI/STY Genes Affect Pre- and Post-meiotic Anther Processes in Auxin Sensing Domains in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.735451openalex-snapshot
Hormonome Dynamics During Microgametogenesis in Different Nicotiana Species
inferred← citeshttps://doi.org/10.3389/fpls.2023.1128911openalex-snapshot
Transcriptomic analysis reveals candidate genes associated with anther development in Lilium Oriental Hybrid ‘Siberia’
inferred← citeshttps://doi.org/10.3390/biom12081149openalex-snapshot
Comparative Transcriptome Analysis Reveals Hormone Signal Transduction and Sucrose Metabolism Related Genes Involved in the Regulation of Anther Dehiscence in Photo-Thermo-Sensitive Genic Male Sterile Wheat
inferred← citeshttps://doi.org/10.3390/genes14030661openalex-snapshot
Identifying Genes Associated with Female Flower Development of Phellodendron amurense Rupr. Using a Transcriptomics Approach
inferred← citeshttps://doi.org/10.3390/horticulturae11040398openalex-snapshot
The Transcription Factor LoTDF1 Plays a Role in Early Anther Development in Lily (Lilium Oriental Hybrids)
inferred← citeshttps://doi.org/10.3390/horticulturae8050365openalex-snapshot
Hormonal Signaling in the Progamic Phase of Fertilization in Plants
inferred← citeshttps://doi.org/10.3390/horticulturae9060665openalex-snapshot
Analysis of YUC and TAA/TAR Gene Families in Tomato
inferred← citeshttps://doi.org/10.3390/ijms20051015openalex-snapshot
Histological and Cytological Characterization of Anther and Appendage Development in Asian Lotus (Nelumbo nucifera Gaertn.)
inferred← citeshttps://doi.org/10.3390/ijms22157907openalex-snapshot
The Rab Geranylgeranyl Transferase Beta Subunit Is Essential for Embryo and Seed Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms241311177openalex-snapshot
Opposite Auxin Dynamics Determine the Gametophytic and Embryogenic Fates of the Microspore
inferred← citeshttps://doi.org/10.3390/plants10112382openalex-snapshot
Two Is Company, but Four Is a Party—Challenges of Tetraploidization for Cell Wall Dynamics and Efficient Tip-Growth in Pollen
inferred← citeshttps://doi.org/10.3390/plants11192640openalex-snapshot
The S-Gene YUC6 Pleiotropically Determines Male Mating Type and Pollen Size in Heterostylous Turnera (Passifloraceae): A Novel Neofunctionalization of the YUCCA Gene Family
inferred← citeshttps://doi.org/10.3390/plants12020286openalex-snapshot
Annotation of the Turnera subulata (Passifloraceae) Draft Genome Reveals the S-Locus Evolved after the Divergence of Turneroideae from Passifloroideae in a Stepwise Manner
inferred← citeshttps://doi.org/10.3390/plants12223804openalex-snapshot
Disruption of the Contents of Endogenous Hormones Cause Pollen Development Obstruction and Abortion in Male-Sterile Hybrid Lily Populations
inferred← citeshttps://doi.org/10.3390/plants13101359openalex-snapshot
The Effect of Different Temperatures on the Viability and Senescence of Plum Ovules (Prunus domestica L.)
inferred← citeshttps://doi.org/10.3390/plants14050749openalex-snapshot
Identity Transitions of Tapetum Phases: Insights into Vesicular Dynamics and in Mortem Support During Pollen Maturation
inferred← citeshttps://doi.org/10.3390/plants14060859openalex-snapshot
Transcriptional Analysis Reveals the Differences in Response of Floral Buds to Boron Deficiency Between Two Contrasting Brassica napus Varieties
inferred← citeshttps://doi.org/10.3390/plants15040664openalex-snapshot
Genome-Wide Analysis of the YUCCA Gene Family in Wheat and the Potential Roles of TaYUCCA19 and Its Homologs in Male Reproductive Development
inferred← citeshttps://doi.org/10.3390/plants9080956openalex-snapshot
First Steps in the Successful Fertilization of Rice and Arabidopsis: Pollen Longevity, Adhesion and Hydration
inferred← citeshttps://doi.org/10.3410/f.732817295.793556725openalex-snapshot
Faculty Opinions recommendation of A Newly Identified Flower-Specific Splice Variant of AUXIN RESPONSE FACTOR8 Regulates Stamen Elongation and Endothecium Lignification in Arabidopsis.
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535746openalex-snapshot
Additional file 1 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535752openalex-snapshot
Additional file 2 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535758openalex-snapshot
Additional file 3 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535761openalex-snapshot
Additional file 4 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535767openalex-snapshot
Additional file 5 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535773openalex-snapshot
Additional file 7 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.6084/m9.figshare.13535776openalex-snapshot
Additional file 8 of Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.